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	321.	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly. [electronic resource] by Halal, F Picard, J L Raymond-Tremblay, D de Bosset, P Producer: 19821216 In: American journal of medical genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	322.	The oral-facial-digital syndromes reviewed: the role of computerized axial tomography in management. [electronic resource] by Jacquemart, C J Trotter, T L Kaplan, A M Beauchamp, R F Producer: 19800625 In: Arizona medicine vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	323.	The contribution of electromyography to the diagnostics of some rare palatal anomalies. [electronic resource] by Velepic, Mitja S Sasso, Antun B Ahel, Vladimir V Starcevic, Radan A Komljenovic, Dean B Velepic, Marko M Producer: 20051018 In: International journal of pediatric otorhinolaryngology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	324.	[A hereditary abnormality as paternity evidence]. [electronic resource] by van der Hagen, Carl Birger Producer: 20070823 In: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	325.	Anesthetic considerations in a parturient with oral-facial-digital syndrome and repaired tetralogy of Fallot with left ventricular dysfunction. [electronic resource] by McKinnie, J E Abdullah, A N Ramanathan, J Producer: 20141209 In: International journal of obstetric anesthesia vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	326.	The oro-facial-digital syndrome. [electronic resource] by Whelan, D T Feldman, W Dost, I Producer: 19760102 In: Clinical genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	327.	Orodigitofacial dysostosis and oculodentodigital dysplasia. Two distinct syndromes with some similarities. [electronic resource] by Eidelman, E Chosack, A Wagner, M L Producer: 19670411 In: Oral surgery, oral medicine, and oral pathology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	328.	[Orofaciodigital syndrome. Clinical features and genetics]. [electronic resource] by Stahl, A Furhmann, W Producer: 19680827 In: Deutsche medizinische Wochenschrift (1946) vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	329.	Four novel mutations in the OFD1 (Cxorf5) gene in Finnish patients with oral-facial-digital syndrome 1. [electronic resource] by Rakkolainen, A Ala-Mello, S Kristo, P Orpana, A Järvelä, I Producer: 20020517 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	330.	Confirmation that mutations in DDX59 cause an autosomal recessive form of oral-facial-digital syndrome: Further delineation of the DDX59 phenotype in two new families. [electronic resource] by Faily, Sara Perveen, Rahat Urquhart, Jill Chandler, Kate Clayton-Smith, Jill Producer: 20171207 In: European journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	331.	Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: a review. [electronic resource] by Odent, S Le Marec, B Toutain, A David, A Vigneron, J Tréguier, C Jouan, H Milon, J Fryns, J P Verloes, A Producer: 19980326 In: American journal of medical genetics vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	332.	Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients. [electronic resource] by Tsurusaki, Y Kosho, T Hatasaki, K Narumi, Y Wakui, K Fukushima, Y Doi, H Saitsu, H Miyake, N Matsumoto, N Producer: 20130805 In: Clinical genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	333.	Detailed clinical, genetic and neuroimaging characterization of OFD VI syndrome. [electronic resource] by Darmency-Stamboul, Véronique Burglen, Lydie Lopez, Estelle Mejean, Nathalie Dean, John Franco, Brunella Rodriguez, Diana Lacombe, Didier Desguerres, Isabelle Cormier-Daire, Valérie Doray, Bérénice Pasquier, Laurent Gonzales, Marie Pastore, Matthew Crenshaw, Melissa L Huet, Frédéric Gigot, Nadège Aral, Bernard Callier, Patrick Faivre, Laurence Attié-Bitach, Tania Thauvin-Robinet, Christel Producer: 20131104 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	334.	Facial comedonal acne in orofaciodigital syndrome type 1 caused by a novel frameshift variant in OFD1. [electronic resource] by Rotunno, R Diociaiuti, A Agolini, E Latorre, S Carnevale, C Novelli, A El Hachem, M Castori, M Producer: 20200115 In: Clinical and experimental dermatology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	335.	Phenotypic heterogeneity among the pilosebaceous dysplasias. [electronic resource] by Solomon, L M Producer: 19760126 In: Modern problems in paediatrics vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	336.	[The orofaciodigital syndrome. The Papillon-Léage-Psaume syndrome]. [electronic resource] by Koberg, W Schettler, D Producer: 19700205 In: Deutsche zahnarztliche Zeitschrift vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	337.	Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features. [electronic resource] by Hedera, Peter Innis, Jeffrey W Producer: 20040422 In: American journal of medical genetics. Part A vol. 122A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	338.	The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation. [electronic resource] by Thauvin-Robinet, Christel Lee, Jaclyn S Lopez, Estelle Herranz-Pérez, Vicente Shida, Toshinobu Franco, Brunella Jego, Laurence Ye, Fan Pasquier, Laurent Loget, Philippe Gigot, Nadège Aral, Bernard Lopes, Carla A M St-Onge, Judith Bruel, Ange-Line Thevenon, Julien González-Granero, Susana Alby, Caroline Munnich, Arnold Vekemans, Michel Huet, Frédéric Fry, Andrew M Saunier, Sophie Rivière, Jean-Baptiste Attié-Bitach, Tania Garcia-Verdugo, Jose Manuel Faivre, Laurence Mégarbané, André Nachury, Maxence V Producer: 20150112 In: Nature genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	339.	[Weill-Marchesani syndrome]. [electronic resource] by Herrera, J Morales, M Producer: 19871216 In: Revista chilena de pediatria vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	340.	Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease. [electronic resource] by Donnai, D Kerzin-Storrar, L Harris, R Producer: 19870520 In: Journal of medical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 531 results.